RS1042821 MSH6

Health Risk Chr 2:47783348 snv missense variant

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What This Variant Does

"CLNSIG=2

Associated Conditions

Hereditary nonpolyposis colorectal neoplasms

Hereditary cancer-predisposing syndrome

Lynch syndrome

Hereditary nonpolyposis colorectal neoplasms

Hereditary cancer-predisposing syndrome

Lynch syndrome

Population Frequencies

gnomAD ALL

18.4%

1kG AFR

79%

1kG ALL

20.1%

1kG AMR

86%

1kG EAS

27.6%

1kG EUR

81.8%

1kG SAS

17.4%

Other Variants in MSH6